A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037475



Internal ID18780006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:77155482..77173657hg38UCSC Ensembl
Innerchr9:79770398..79788573hg19UCSC Ensembl
Innerchr9:78960218..78978393hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3818176
hg1918176
hg1818176
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7682n100
Supporting Variantsnssv3696389, nssv3696388
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037475
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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